RT Book, Section A1 Bissonnette, Bruno A1 Luginbuehl, Igor A1 Engelhardt, Thomas SR Print(0) ID 1164085441 T1 Smith-Magenis Syndrome T2 Syndromes: Rapid Recognition and Perioperative Implications, 2e YR 2019 FD 2019 PB McGraw-Hill Education PP New York, NY SN 9781259861789 LK accesspediatrics.mhmedical.com/content.aspx?aid=1164085441 RD 2022/08/11 AB A syndrome of multiple congenital anomalies characterized by midface hypoplasia, broad face, hearing loss (conductive and/or sensorineural), congenital heart defect, hypothyroidism, severe scoliosis, brachydactyly, and decreased pain sensitivity but peripheral neuropathy. Severe behavior problems (biting and head banging) and sleep disturbances.